Canonical Allele Identifier: CA1012882546

Gene: EPHX1

Linked Data

• dbSNP Id: rs1667630635
• gnomAD v3: 1-225831967-T-C
• gnomAD v4: 1-225831967-T-C

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.225831967T>C , CM000663.2:g.225831967T>C	GRCh38
NC_000001.10:g.226019668T>C , CM000663.1:g.226019668T>C	GRCh37
NC_000001.9:g.224086291T>C	NCBI36
NG_009776.1:g.26872T>C

Transcript Alleles

HGVS	Amino-acid change
ENST00000272167.10:c.364+8T>C MANE Select	ENSP00000272167.5:n.364+8T>C
ENST00000272167.9:c.364+8T>C	ENSP00000272167.5:n.364+8T>C
ENST00000366837.5:c.364+8T>C	ENSP00000355802.4:n.364+8T>C
ENST00000445856.5:c.364+8T>C	ENSP00000398491.1:n.364+8T>C
ENST00000448202.5:c.364+8T>C	ENSP00000408469.1:n.364+8T>C
ENST00000467015.1:n.259T>C
ENST00000614058.4:c.364+8T>C	ENSP00000480004.1:n.364+8T>C
NM_000120.3:c.364+8T>C	NP_000111.1:n.364+8T>C
NM_001136018.3:c.364+8T>C	NP_001129490.1:n.364+8T>C
NM_001291163.1:c.364+8T>C	NP_001278092.1:n.364+8T>C
NM_000120.4:c.364+8T>C	NP_000111.1:n.364+8T>C
NM_001136018.4:c.364+8T>C MANE Select	NP_001129490.1:n.364+8T>C
NM_001291163.2:c.364+8T>C	NP_001278092.1:n.364+8T>C
NM_001378426.1:c.364+8T>C	NP_001365355.1:n.364+8T>C
NM_001378427.1:c.364+8T>C	NP_001365356.1:n.364+8T>C
NM_001378428.1:c.337+8T>C	NP_001365357.1:n.337+8T>C
NM_001378429.1:c.364+8T>C	NP_001365358.1:n.364+8T>C
NM_001378430.1:c.364+8T>C	NP_001365359.1:n.364+8T>C
NM_001378431.1:c.364+8T>C	NP_001365360.1:n.364+8T>C
NM_001378432.1:c.364+8T>C	NP_001365361.1:n.364+8T>C
NR_165624.1:n.369+54T>C
NR_165625.1:n.415+8T>C
NR_165626.1:n.861+8T>C
NR_165627.1:n.560+8T>C